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snowball effect of RNA binding protein dysfunction in amyotrophic lateral
sclerosis. Freischmidt, A. Frey, D. Early and selective loss of neuromuscular
synapse subtypes with low sprouting competence in motoneuron diseases. Fried, L.
Untangling the concepts of disability, frailty, and comorbidity: implications
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distinguished by expression of transcription factor Err3. Fryer, H. Excitotoxic
death of a subset of embryonic rat motor neurons in vitro. Fu, H. Selective
vulnerability in neurodegenerative diseases.

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internuclear neurons in the monkey abducens nucleus. Fujimura-Kiyono, C. Onset
and spreading patterns of lower motor neuron involvements predict survival in
sporadic amyotrophic lateral sclerosis. Fujita, K. Decreased cytochrome c
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activities in the spinal cords of patients with amyotrophic lateral sclerosis.

Fujita, S. Origin of brain macrophages and the nature of the so-called
microglia.

Mitochondria, motor neurons and aging. Gardiner, P. Physiological properties of
motoneurons innervating different muscle unit types in rat gastrocnemius.
Gargiulo-Monachelli, G. Regional spread pattern predicts survival in patients
with sporadic amyotrophic lateral sclerosis. Georgopoulos, A. On the relations
between the direction of two-dimensional arm movements and cell discharge in
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IL controls early microglial phenotypes and disease onset in als caused by
misfolded superoxide dismutase 1. Greenway, M. Resistance to glycogen depletion
of motor units in the cat rectus lateralis muscle. Gulino, R. TDP as a modulator
of synaptic plasticity in a mouse model of spinal motoneuron degeneration. CNS
Neurol. Drug Targets 14, 55— Gurney, M. The use of transgenic mouse models of
amyotrophic lateral sclerosis in preclinical drug studies.

Motor neuron degeneration in mice that express a human Cu,Zn superoxide
dismutase mutation. Gustafsson, B. Hadzipasic, M. Haenggeli, C. Hall, C.
Progressive motor neuron pathology and the role of astrocytes in a human stem
cell model of vcp-related ALS. Hall, E. Relationship of oxygen radical-induced
lipid peroxidative damage to disease onset and progression in a transgenic model
of familial ALS. Harms, M. Lack of C9ORF72 coding mutations supports a gain of
function for repeat expansions in amyotrophic lateral sclerosis.

Harris, J.

Synaptic energy use and supply. Neuron 75, — Hashizume, K. Medial gastrocnemius
motor nucleus in the rat: age-related changes in the number and size of
motoneurons. He, C. Expression of peripherin in ubiquinated inclusions of
amyotrophic lateral sclerosis. Hedlund, E. Global gene expression profiling of
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and pathways of degeneration and protection.

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model of amyotrophic lateral sclerosis.


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marrow-derived and present antigen in vivo. Hideyama, T. Higelin, J. Hill, S.
Hira, R. In vivo optogenetic tracing of functional corticocortical connections
between motor forelimb areas. Hirano, A. Fine structural study of
neurofibrillary changes in a family with amyotrophic lateral sclerosis.
Hochstim, C. Identification of positionally distinct astrocyte subtypes whose
identities are specified by a homeodomain code. Cell , — Hossaini, M.

Spinal inhibitory interneuron pathology follows motor neuron degeneration
independent of glial mutant superoxide dismutase 1 expression in SOD1-ALS Mice.
Hsiung, G. Clinical and pathological features of familial frontotemporal
dementia caused by C9ORF72 mutation on chromosome 9p. Huang, C. Profiling the
genes affected by pathogenic TDP in astrocytes. Entorhinal cortical neurons are
the primary targets of FUS mislocalization and ubiquitin aggregation in FUS
transgenic rats. Huber, A. Distinct roles for secreted semaphorin signaling in
spinal motor axon guidance.

Neuron 48, — Hugon, J.


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check the accommodation option s breakdown on this page. What is there to do at
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